Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Pyridine → n-Fmoc-o-t-butyl-l-serinyl fluoride
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Pyridine | HCID 1049 | — |
| 반응물 | Cyanuric fluoride | HCID 12664 | — |
| 반응물 | N-(9-Fluorenylmethoxycarbonyl)-O-tert-butylserine | HCID 2724633 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | n-Fmoc-o-t-butyl-l-serinyl fluoride | HCID 11315144 | — |
반응 단계
N-FMOC-O-t-Butyl-L-serine (10 g, 26.07 mmol) (Bachem) was dissolved in dichloromethane (135 mL). Pyridine (2.11 mL, 26.07 mmol) (Aldrich) and cyanuric fluoride (3.52 g, 26.07 mmol) (Aldrich) were successively added at room temperature and the mixture was stirred overnight. Ice cold water (100 mL) was added and the resulting slurry was filtered. The filtrate was poured into a separatory funnel and the layers were separated. The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to afford N-FMOC-O-t-butyl-L-serinyl fluoride as a colorless oil which solidified upon standing. (Yield 9.79 g., 97%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07084270B2 |
| 출처 데이터셋 | uspto-grants-2006_08 |
| ORD ID | ord-7e467cb3ee834f5c8c6a348a4e446e43 |
| 출처 메모 | uspto-grants-2006_08 |